Castanea crenata

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

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Distribution

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Scientific Literature

Phytochemical Profile

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Details Top

Internal ID	UUID64402a7b4c19d260045836
Scientific name	Castanea crenata
Authority	Siebold & Zucc.
First published in	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 224 (1846)

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Synonyms Top

Scientific name	Authority	First published in
Castanea crenata f. gigantea	Makino	J. Jap. Bot. 3: 14 1926
Castanea crenata var. femina	Makino	J. Jap. Bot. 3: 14. 1926
Castanea crenata var. imperfecta	Makino	J. Jap. Bot. 5: 44. 1928
Castanea crenata var. microcarpa	Makino	Ill. Fl. Nippon 655. 1940
Castanea crenata var. pleiocarpa	Makino	J. Jap. Bot. 3: 14. 1926
Castanea crenata var. syakacephala	Makino	J. Jap. Bot. 6: 26. 1929
Castanea crenata var. caudata	Miyoshi	Proc. Imp. Acad. Japan 3: 238. 1927
Castanea crenata var. dulcis	Nakai	Index Seminum (TI, Tokyo) 1934: 11.
Castanea crenata var. pulchella	Honda	Bot. Mag. (Tokyo) 57: 107. 1943
Castanea crenata f. femina	(Makino) Sugim.	New Keys Jap. Trees 458 1961
Castanea crenata f. imperfecta	(Makino) Sugim.	New Keys Jap. Trees 458 1961
Castanea crenata f. pleiocarpa	(Makino) Sugim.	New Keys Jap. Trees 458 1961
Castanea crenata f. pulchella	(Honda) Sugim.	New Keys Jap. Trees 458 1961
Castanea crenata f. syakacephala	(Makino) Sugim.	New Keys Jap. Trees 458 1961
Castanea crenata f. pendula	(Miyoshi) Sugim.	New Keys Jap. Trees 458 1961
Castanea crenata var. kawasei	Sugim.	J. Geobot. 16: 49. 1968
Castanea castanea var. pubinervis	Sarg.	Silva 9: 9. 1896
Castanea chinensis	Hassk.	Cat. Hort. Bot. Bogor. Alt. : 73 (1844)
Castanea crenata var. canescens	(Blume) Koidz.	Bot. Mag. (Tokyo) 40: 339 1926
Castanea crenata var. elongata	(Blume) A.Camus	Chataigniers Texte: 192 1929
Castanea crenata var. japonica	(Blume) Koidz.	Bot. Mag. (Tokyo) 40: 339. 1926
Castanea crenata var. kusakuri	Nakai	Bot. Mag. (Tokyo) 45: 112. 1931 [20 Mar 1931]
Castanea crenata var. longispina	(Blume) A.Camus	Chataigniers Texte: 192 1929
Castanea crenata var. obtexta	(Blume) A.Camus	Chataigniers Texte: 192 1929
Castanea crenata var. ookasi	(Blume) A.Camus	Chataigniers Texte: 192 1929
Castanea crenata var. pendula	Miyoshi	Bot. Mag. (Tokyo) 33: 187. 1919
Castanea crenata var. quercina	(Blume) A.Camus	Chataigniers Texte: 192 1929
Castanea crenata var. siba-kuri	(Blume) A.Camus	Chataigniers Texte: 192 1929
Castanea crenata var. stricta	(Siebold & Zucc.) A.Camus	Chataigniers Texte: 191. 1929
Castanea crenata var. tamba	A.Camus	Chataigniers Texte: 193. 1929
Castanea japonica	Blume	Mus. Bot. 1: 284 (1851)
Castanea japonica var. canescens	Blume	Mus. Bot. 1: 286. 1851
Castanea japonica var. elongata	Blume	Ann. Mus. Bot. Lugduno-Batavi 1: 286. 1864
Castanea japonica var. kusakuri	Blume	Mus. Bot. 1: 285. 1851
Castanea japonica var. longispina	Blume	Ann. Mus. Bot. Lugduno-Batavi 1: 285. 1864
Castanea japonica var. obtexta	Blume	Ann. Mus. Bot. Lugduno-Batavi 1: 286. 1864
Castanea japonica var. ookasi	Blume	Mus. Bot. 1: 285. 1851
Castanea japonica var. quercina	Blume	Ann. Mus. Bot. Lugduno-Batavi 1: 285. 1864
Castanea japonica var. siba-kuri	Blume	Ann. Mus. Bot. Lugduno-Batavi 1: 286. 1864
Castanea japonica var. stricta	(Siebold & Zucc.) Blume	Mus. Bot. 1: 286. 1851
Castanea kusakuri	Koidz.	Bot. Mag. (Tokyo) 40: 337 (1926)
Castanea pubinervis	C.K.Schneid.	Ill. Handb. Laubholzk. 1: 158. 1904 (1904)
Castanea sativa var. pubinervis	(C.K.Schneid.) Makino	Bot. Mag. (Tokyo) 23: 12. 1909
Castanea stricta	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 225 (1846)
Castanea vulgaris var. elongata	A.DC.	Prodr. [A. P. de Candolle] 16(2): 115. 1864
Castanea vulgaris var. japonica	(Blume) A.DC.	Prodr. [A. P. de Candolle] 16(2): 115. 1864
Castanea vulgaris var. kusakuri	(Blume) A.DC.	Prodr. 16(2): 115 1864
Castanea vulgaris var. subdentata	A.DC.	Prodr. [A. P. de Candolle] 16(2): 115. 1864
Castanea sativa var. japonica	(Blume) Seemen	Bot. Jahrb. Syst. 29: 287. 1900

Common names Top

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Filter by language:

Language	Common/alternative name
English	japanese chestnut
Spanish	castano japones
Spanish	castano japonés
Spanish	castaño japones
Spanish	castaño japonés
Bulgarian	японски кестен
Catalan	castanyer japonès
German	japanische kastanie
Basque	japoniar gaztainondo
Persian	شاهبلوط ژاپنی
French	chataignier crenele
French	châtaignier crénelé
French	châtaignier du japon
French	châtaignier japonais
Galician	castiñeiro do xapón
Croatian	japanski kesten
Japanese	くり
Japanese	栗
Japanese	クリ
Korean	밤나무
Korean	밤나무꽃
Latvian	japānas kastaņa
Malayalam	കൊറിയൻ ചെസ്റ്റ്നട്ട്
Norwegian Bokmål	japankastanje
Polish	kasztan japoński
Russian	Каштан городчатый
Russian	Японский каштан
Russian	Каштан японский
Slovenian	japonski kostanj
Thai	เกาลัดญี่ปุ่น
Turkish	japon kestanesi
Ukrainian	Каштан японський
Chinese	茅栗
Chinese	栗子
Chinese	日本栗
Chinese	日本板栗

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Eastern Asia
  - Japan
  - Korea

Europe click to expand
- Southeastern Europe
  - Italy
- Southwestern Europe
  - Portugal
  - Spain

Northern America click to expand
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000811268
UNII	K5V65F158O
Florida Plant Atlas	230
USDA Plants	CACR27
Tropicos	13100497
INPN	89302
KEW	urn:lsid:ipni.org:names:30319741-2
The Plant List	kew-34949
Missouri Botanical Garden	280773
PaleoBotany	53554
Open Tree Of Life	429760
Observations.org	116082
NCBI Taxonomy	103480
NBN Atlas	NBNSYS0200003449
IUCN Red List	62004433
IPNI	30319741-2
iNaturalist	122786
GBIF	5333249
Freebase	/m/0dtcfl
EPPO	CSNCR
EOL	1148515
USDA GRIN	9434
Wikipedia	Castanea_crenata
CMAUP	NPO5303

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_020976635.1	NIFoS_Ccrenata_1.0	Scaffold	National Institute of Forest Science, South Korea	2021-11-24	100.0x	729.54 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Damage analysis of Pochazia shantungensis (Hemiptera: Ricaniidae) in persimmons

Baek S, Lee G, Park CG

PLoS One

16-Apr-2024

PMCID:	PMC11020831
doi:	10.1371/journal.pone.0301471
PMID:	38625892

Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity

Gao XY, Li XY, Zhang CY, Bai CY

Front Pharmacol

23-Feb-2024

PMCID:	PMC10923241
doi:	10.3389/fphar.2024.1268464
PMID:	38464713

Anti-Inflammatory Effect of Chestnut Honey and Cabbage Mixtures Alleviates Gastric Mucosal Damage

Kim HJ, Jin BR, Lee CD, Kim D, Lee AY, Lee S, An HJ

Nutrients

29-Jan-2024

PMCID:	PMC10857084
doi:	10.3390/nu16030389
PMID:	38337674

Chromosome-scale genome assembly of sweet tea (Lithocarpus polystachyus Rehder)

Liu H, Zhang R, Zhou BF, Shen Z, Chen XY, Gao J, Wang B

Sci Data

06-Dec-2023

PMCID:	PMC10700502
doi:	10.1038/s41597-023-02791-y
PMID:	38057329

Factors influencing the difference in dissolved ion inputs to the forest floor between deciduous and coniferous stands: comparison under high and low atmospheric deposition conditions

Imamura N, Ohte N, Tanaka N

Environ Monit Assess

02-Dec-2023

PMCID:	PMC10693530
doi:	10.1007/s10661-023-12132-6
PMID:	38041704

The emerging role of medical foods and therapeutic potential of medical food-derived exosomes

Hur JY, Lee S, Shin WR, Kim YH, Ahn JY

Nanoscale Adv

11-Nov-2023

PMCID:	PMC10729880
doi:	10.1039/d3na00649b
PMID:	38125597

Cryphonectria parasitica Detections in England, Jersey, and Guernsey during 2020–2023 Reveal Newly Affected Areas and Infections by the CHV1 Mycovirus

Romon-Ochoa P, Samal P, Gorton C, Lewis A, Chitty R, Eacock A, Krzywinska E, Crampton M, Pérez-Sierra A, Biddle M, Jones B, Ward L

J Fungi (Basel)

20-Oct-2023

PMCID:	PMC10607933
doi:	10.3390/jof9101036
PMID:	37888292

How much do field mice prefer dwarf bamboo seeds? Two‐choice experiments between seeds of Sasa borealis and several tree species on the forest floor

Suzuki H, Kajimura H

Ecol Evol

19-Oct-2023

PMCID:	PMC10587390
doi:	10.1002/ece3.10636
PMID:	37869436

The nuclear factor erythroid 2-related factor 2/p53 axis in breast cancer

Xia L, Ma W, Afrashteh A, Sajadi MA, Fakheri H, Valilo M

Biochem Med (Zagreb)

15-Oct-2023

PMCID:	PMC10564154
doi:	10.11613/BM.2023.030504
PMID:	37841775

Phytophthora : taxonomic and phylogenetic revision of the genus

Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ

Stud Mycol

06-Oct-2023

PMCID:	PMC10825748
doi:	10.3114/sim.2023.106.05
PMID:	38298569

Cryphonectria carpinicola discovered in Japan: first report of the sexual state on Carpinus tree

Cornejo C, Otani T, Suzuki N, Beenken L

Mycoscience

30-Sep-2023

PMCID:	PMC10627740
doi:	10.47371/mycosci.2023.07.001
PMID:	37936945

Identification and Quantification of the Major Phenolic Constituents in Castanea sativa and Commercial Interspecific Hybrids (C. sativa x C. crenata) Chestnuts Using HPLC–MS/MS

Medic A, Kunc P, Zamljen T, Hudina M, Veberic R, Solar A

Int J Mol Sci

23-Aug-2023

PMCID:	PMC10488303
doi:	10.3390/ijms241713086
PMID:	37685892

Castanea crenata honey reduces influenza infection by activating the innate immune response

Kwon EB, Kim SG, Kim YS, Kim B, Han SM, Lee HJ, Choi HM, Choi JG

Front Immunol

22-Aug-2023

PMCID:	PMC10497975
doi:	10.3389/fimmu.2023.1157506
PMID:	37711616

Commodity risk assessment of Fagus sylvatica plants from the UK

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P

EFSA J

28-Jul-2023

PMCID:	PMC10375364
doi:	10.2903/j.efsa.2023.8118
PMID:	37522095

Low Allergenicity in Processed Wheat Flour Products Using Tannins from Agri-Food Wastes

Tsurunaga Y, Arima S, Kumagai S, Morita E

Foods

17-Jul-2023

PMCID:	PMC10378952
doi:	10.3390/foods12142722
PMID:	37509814

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Harmala alkaloids
Flazin	5377686	Click to see C1=CC=C2C(=C1)C3=CC(=NC(=C3N2)C4=CC=C(O4)CO)C(=O)O	308.29	unknown	via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
5-Methoxycanthin-6-one	259218	Click to see COC1=CC2=NC=CC3=C2N(C1=O)C4=CC=CC=C34	250.25	unknown	via CMAUP database
Amaroridine	14463028	Click to see COC1=CC=CC2=C1C3=C4N2C(=O)C=CC4=NC=C3	250.25	unknown	via CMAUP database
Bruceolline B	190940	Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C(=CC4=NC=C3)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O	560.50	unknown	via CMAUP database
Canthin-6-one	97176	Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3	220.23	unknown	via CMAUP database
Canthin-6-one N-oxide	9991699	Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=[N+](C=C3)[O-]	236.22	unknown	via CMAUP database
Picrasidine Q	54714262	Click to see COC1=C(C2=NC=CC3=C2N(C1=O)C4=CC=CC=C34)O	266.25	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-(3,4,5-trihydroxybenzoyl)oxyoxolan-3-yl]methyl 3,4,5-trihydroxybenzoate	163022993	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O)O	484.40	unknown	https://doi.org/10.1248/CPB.32.483
[(2R,3R,4R,5R)-3,4,5-trihydroxy-4-(hydroxymethyl)oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate	163034776	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(CO)O)O	332.26	unknown	https://doi.org/10.1248/CPB.32.483
[(2R,3R,4R,5R)-3,4,5-trihydroxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate	92238311	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.44.2236 https://doi.org/10.1248/CPB.32.483
[(2R,3R,4R,5R)-3,5-dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate	162951152	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O	636.50	unknown	https://doi.org/10.1080/00021369.1984.10866332
[(2R,3R,4R,5R)-4,5-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate	102157672	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	636.50	unknown	https://doi.org/10.1248/CPB.32.483
[(2R,3R,4R,5S)-3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate	163031229	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)(COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O	636.50	unknown	https://doi.org/10.1248/CPB.32.483
1,2'-Di-O-galloylhamamelofuranose	131752619	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O)O	484.40	unknown	https://doi.org/10.1248/CPB.32.483
1,2',5-Tri-O-galloylhamamelofuranose	131752620	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)(COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O	636.50	unknown	https://doi.org/10.1248/CPB.32.483
2,2',5-Tri-O-galloylhamamelofuranose	131752621	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O	636.50	unknown	https://doi.org/10.1271/BBB1961.48.1411 https://doi.org/10.1080/00021369.1984.10866332
2',5-Digalloylhamamelofuranose	16211077	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.44.2236 https://doi.org/10.1248/CPB.32.483
5-O-Galloylhamamelofuranose	131752618	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(CO)O)O	332.26	unknown	https://doi.org/10.1248/CPB.32.483
Hamamelitannin	253775	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.44.2236
Hamamelofuranose 2'5'-digallate	44584241	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O	484.40	unknown	https://doi.org/10.1248/CPB.44.2236 https://doi.org/10.1248/CPB.32.483
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol, (+)-	160521	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Coumarinolignans
(2S,3S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one	24970879	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO	416.40	unknown	via CMAUP database
9H-Pyrano(2,3-f)-1,4-benzodioxin-9-one, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-, trans-(+-)-	11982428	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O	386.40	unknown	via CMAUP database
Cleomiscosin A	442510	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O	386.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Flavonolignans
2-[(2S,3S)-2,3-Dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-1,4-benzodioxin-6-yl]-5,7-dihydroxy-4H-1-benzopyran-4-one	44582381	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O	464.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Epipinoresinol	637584	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
Medioresinol	181681	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC	388.40	unknown	via CMAUP database
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Hexadecanoic acid, 8-hydroxy-, (S)-	5312819	Click to see CCCCCCCCC(CCCCCCC(=O)O)O	272.42	unknown	via CMAUP database
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid	2266	Click to see C(CCCC(=O)O)CCCC(=O)O	188.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,3-diacylglycerols
1,3-Diolein	5497165	Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCCCCCCCC)O	621.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cucumegastigmane I	16105430	Click to see CC1=CC(=O)CC(C1(C=CC(CO)O)O)(C)C	240.29	unknown	via CMAUP database
Vomifoliol	5280462	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,11,12,15,16-hexahydroxy-17-(hydroxymethyl)-9,13-dimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one	5315511	Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O)O	428.40	unknown	via CMAUP database
(1R,2R,3R,6R,8S,12S,13S,14R,15R,16S,17R,19S)-2,3,12,15,16,19-hexahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione	11304852	Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5O)C)O)O)C)O	426.40	unknown	via CMAUP database
(1R,2R,3R,6R,8S,9R,10R,11S,12R)-2,3,10,11-tetrahydroxy-8,12-dimethyl-8-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-5,13-dioxatetracyclo[7.5.0.01,6.02,12]tetradecan-4-one	21769824	Click to see CC1=CC(=O)OC1C2(CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C	396.40	unknown	via CMAUP database
(1R,2S,3R,6R,8R,13S,14R,15R,16S,17R)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylic acid	10391474	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)O)O)O)C)O	506.50	unknown	via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid	10556620	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)O	696.70	unknown	via CMAUP database
[1,3,3abeta,4,5,6abeta,7,7aalpha,10,11,11a,11balpha-Dodecahydro-1beta,2alpha,3abeta,4beta,11beta-pentahydroxy-3,8,11abeta-trimethyl-5-oxo-2H-3beta,11cbeta-(epoxymethano)phenanthro[10,1-bc]pyran-10alpha-yl]beta-D-glucopyranoside	101273517	Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O	574.60	unknown	via CMAUP database
15-O-(3-Methylbutanoyl)-3-O-beta-D-glucopyranosylbruceolide	21636147	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	684.70	unknown	via CMAUP database
3-Ethyl-4-hydroxy-4-methyl-2-pentenoic acid (1R)-1,2,3,3abeta,4,5,6abeta,7,7aalpha,8,9,11a,11balpha,11c-tetradecahydro-1beta,2alpha-dihydroxy-10-(beta-D-glucopyranosyloxy)-3-(methoxycarbonyl)-8alpha,11abeta-dimethyl-5,9-dioxo-3beta,11cbeta-(epoxymethano)phenanthro[10,1-bc]pyran-4beta-yl ester	11227971	Click to see CCC(=CC(=O)OC1C2C34COC2(C(C(C3C5(C=C(C(=O)C(C5CC4OC1=O)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC)C(C)(C)O	740.70	unknown	via CMAUP database
Bruceantin	5281304	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O	548.60	unknown	via CMAUP database
Bruceantinol	5281305	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)O	606.60	unknown	via CMAUP database
Bruceantinol A	23656477	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)O)O)O)C)O	592.60	unknown	via CMAUP database
Bruceene	101600137	Click to see CC12C(CC3C45C1C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C(=C)C=CC2O	394.40	unknown	via CMAUP database
Brucein D	441788	Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O	410.40	unknown	via CMAUP database
Bruceine A	160006	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)O	522.50	unknown	via CMAUP database
Bruceine B	161496	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C)(OC5)C(=O)OC)O)O)C)O	480.50	unknown	via CMAUP database
Bruceine C	5315509	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)O)(OC5)C(=O)OC)O)O)C)O	564.60	unknown	via CMAUP database
Bruceine E	5315510	Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O)O	412.40	unknown	via CMAUP database
Bruceine G	102059835	Click to see CC1=CC(=O)CC2(C1C(C3C45C2C(C(C(C4C(C(=O)O3)O)(OC5)C)O)O)O)C	394.40	unknown	via CMAUP database
bruceine J	23656476	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)O)O)O)C)O	508.50	unknown	via CMAUP database
Bruceolide	99531	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)O)(OC5)C(=O)OC)O)O)C)O	438.40	unknown	via CMAUP database
Bruceoside A	441789	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	682.70	unknown	via CMAUP database
bruceosideB	3000796	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	682.70	unknown	via CMAUP database
Brusatol	73432	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)O	520.50	unknown	via CMAUP database
butyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate	10556847	Click to see CCCCOC(=O)C12C3C(C(=O)OC4C3(CO1)C(C(C2O)O)C5(C=C(C(=O)C(C5C4)C)OC6C(C(C(C(O6)CO)O)O)O)C)OC(=O)C=C(C)C	724.70	unknown	via CMAUP database
CID 11765370	11765370	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	710.70	unknown	via CMAUP database
CID 21606956	21606956	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	710.70	unknown	via CMAUP database
CID 3000798	3000798	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	642.60	unknown	via CMAUP database
CID 3000803	3000803	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)CC(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)O	670.70	unknown	via CMAUP database
Dehydrobruceantinol	54604632	Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC	604.60	unknown	via CMAUP database
Dehydrobruceine A	21125878	Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)CC(C)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC	520.50	unknown	via CMAUP database
Dehydrobruceine B	101967133	Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC	478.40	unknown	via CMAUP database
Dehydrobrusatol	59087297	Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC	518.50	unknown	via CMAUP database
Desmrthyl-bruceantinoside A	21606955	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)O	696.70	unknown	via CMAUP database
Javanicolide C	11214625	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(CC(C1O)O)C)O)O)C(=O)OC	524.60	unknown	via CMAUP database
Javanicolide D	11455840	Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)O)(OC5)C(=O)OC)O)O)C)O)O	566.60	unknown	via CMAUP database
Javanicolide E	70686049	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(CC(=O)C1O)C)O)O)C(=O)OC	522.50	unknown	via CMAUP database
Javanicoside B	11169907	Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	684.70	unknown	via CMAUP database
Javanicoside C	11169890	Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	680.60	unknown	via CMAUP database
Javanicoside F	11445415	Click to see CCC(=CC(=O)OC1C2C34COC2(C(C(C3C5(C=C(C(=O)C(C5CC4OC1=O)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC)C	696.70	unknown	via CMAUP database
Javanicoside G	12086835	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(CO6)O)O)O)C)O)O)C(=O)OC	652.60	unknown	via CMAUP database
Javanicoside H	12086836	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(CO6)O)O)O)C)O)O)C(=O)OC	738.70	unknown	via CMAUP database
Javanicoside I	11445340	Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	682.70	unknown	via CMAUP database
Javanicoside K	11479645	Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)O)(OC5)C(=O)OC)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O	728.70	unknown	via CMAUP database
Methyl (1R,2R,6S,7R,8R,13R,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-7-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate	21115217	Click to see CC1=C(C(=O)CC2(C1C(C3C45C2C(C(C(C4CC(=O)O3)(OC5)C(=O)OC)O)O)OC(=O)C=C(C)C)C)OC6C(C(C(C(O6)CO)O)O)O	682.70	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-(3,4-dimethylpent-2-enoyloxy)-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate	441786	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O	548.60	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-acetyloxy-15,16-dihydroxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate	21636148	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	642.60	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-benzoyloxy-15,16-dihydroxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate	11411443	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(OC5)C(=O)OC)O)O)C)OC7C(C(C(C(O7)CO)O)O)O	704.70	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate	101659160	Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O	684.70	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-3-acetyloxy-12,15,16-trihydroxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate	101659159	Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C)(OC5)C(=O)OC)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O	644.60	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate	11490891	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	682.70	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10R,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate	101499202	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(CC(=O)C1O)C)O)O)C(=O)OC	608.60	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10S,11R,13S,14R,15R,16S,17S)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate	11250992	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(CC(C1O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	686.70	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate	101659161	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	768.80	unknown	via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate	101659164	Click to see CC1C=C(C(=O)C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	710.70	unknown	via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-[(4-hydroxy-3,4-dimethyl-1-oxo-2-pentenyl)oxy]-3,16-dioxo-, methyl ester, [11beta,12alpha,15beta(E)]-	101659158	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)O)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	726.70	unknown	via CMAUP database
yadanziolide A	10320238	Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O	426.40	unknown	via CMAUP database
Yadanziolide B	11744055	Click to see CC1=CC(=O)C(C2(C1C(C3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)O)C)O	442.40	unknown	via CMAUP database
Yadanziolide C	10409280	Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O	410.40	unknown	via CMAUP database
Yadanzioside H	101659162	Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O	686.70	unknown	via CMAUP database
Yadanzioside J	101659163	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)CC(C)(C)O)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	700.70	unknown	via CMAUP database
Yadanzioside K	14060346	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	768.80	unknown	via CMAUP database
Yadanzioside M	21115200	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(C(C(C5C2(C=C(C1=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)C(=O)OC	704.70	unknown	via CMAUP database
Yadanzioside O	10417797	Click to see CCC(=CC(=O)OC1C2C34COC2(C(C(C3C5(C=C(C(=O)C(C5CC4OC1=O)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC)C(C)(C)OC(=O)C	782.80	unknown	via CMAUP database
YadanziosideA	101659157	Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)CC(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC	684.70	unknown	via CMAUP database
Yadazioside L	21636149	Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)O)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O	726.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6R,7Z,10E,11aR)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate	49799780	Click to see CC1=CC2C(C(CC(C=CC1=O)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2	348.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Macedonic acid	193076	Click to see CC1(C2CCC3(C(C2(CCC1O)C)C=CC4=C5CC(C(CC5(CCC43C)C)O)(C)C(=O)O)C)C	470.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(5R,7R,8R,9R,10R,13S,17S)-17-[(2S,3S,5R)-5-[(2S)-3,3-dimethyloxiran-2-yl]-2-methoxyoxolan-3-yl]-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate	10414931	Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC)C6C(O6)(C)C)C)C)(C)C	540.70	unknown	via CMAUP database
[(5R,7R,8R,9R,10S,11R,13S,17S)-17-[(2S,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-11-hydroxy-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate	71544782	Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(CC3O)C)C5CC(OC5OC)C(C(C)(C)O)O)C)C)(C)C	574.70	unknown	via CMAUP database
1,2-Dihydrobruceajavanin A	10076750	Click to see CC(=O)OC1CC2C(C(=O)CCC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C)C)(C)C	570.80	unknown	via CMAUP database
Bruceajavanin A	10030889	Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C)C)(C)C	568.70	unknown	via CMAUP database
Bruceajavanone A	44582338	Click to see CCCCCC(=O)OC1CC2(C(CC=C2C3(C1C4(C=CC(=O)C(C4CC3O)(C)C)C)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C	640.80	unknown	via CMAUP database
Bruceajavanone A 7-acetate	44582339	Click to see CCCCCC(=O)OC1CC2(C(CC=C2C3(C1C4(C=CC(=O)C(C4CC3OC(=O)C)(C)C)C)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C	682.90	unknown	via CMAUP database
Bruceajavanone B	44582340	Click to see CC=C(C)C(=O)OC1CC2(C(CC=C2C3(C1C4(C=CC(=O)C(C4CC3OC(=O)C)(C)C)C)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C	666.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
6-Deoxocastasterone	13870433	Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CCC4C3(CC(C(C4)O)O)C)C)O)O	450.70	unknown	https://doi.org/10.1016/S0031-9422(00)83445-7
Castasterone	133534	Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O	464.70	unknown	https://doi.org/10.1271/BBB1961.47.655 https://doi.org/10.1016/S0031-9422(00)83445-7 https://doi.org/10.1016/S0021-9673(01)93583-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Brassinolides and derivatives
Brassinolide	115196	Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O	480.70	unknown	https://doi.org/10.1016/S0031-9422(00)83445-7 https://doi.org/10.1016/S0021-9673(01)93583-6 https://doi.org/10.1271/BBB1961.47.655
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4S,5S)-2-[[(3S,8S,9S,10R,13S,14S,17S)-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol	101916318	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(CO5)O)O)O)C)C)O	450.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
2-[(1R,2S,3R,6R,8S,9S,10R,11R,12S,13S)-11,12-dihydroxy-13-methoxycarbonyl-8-[(2S)-1-methoxy-1-oxopropan-2-yl]-9-methyl-3-(3-methylbut-2-enoyloxy)-4-oxo-5,14-dioxatetracyclo[8.5.0.01,6.02,13]pentadecan-9-yl]acetic acid	70692363	Click to see CC(C1CC2C34COC(C3C(C(=O)O2)OC(=O)C=C(C)C)(C(C(C4C1(C)CC(=O)O)O)O)C(=O)OC)C(=O)OC	568.60	unknown	via CMAUP database
Javanic Acid A	70694422	Click to see CC(C1CC2C34COC(C3C(C(=O)O2)OC(=O)C=C(C)C)(C(C(C4C1(C)CC(=O)O)O)O)C(=O)OC)C(=O)O	554.50	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(2R,3R,4R,5R)-4-hydroxy-3,5-bis[(3,4,5-trihydroxybenzoyl)oxy]-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate	163019436	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)(COC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1248/CPB.32.483
1,2',3,5-Tetra-O-galloylhamamelofuranose	131752622	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)(COC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1248/CPB.32.483
Bruceanic Acid E	70681802	Click to see CC(=CC(=O)OC1C2C34COC2(C(C(C3C(C(CC4OC1=O)C(=O)C)(C)CC(=O)O)O)O)C(=O)OC)C	524.50	unknown	via CMAUP database
Bruceanic Acid E Methyl Ester	70688171	Click to see CC(=CC(=O)OC1C2C34COC2(C(C(C3C(C(CC4OC1=O)C(=O)C)(C)CC(=O)OC)O)O)C(=O)OC)C	538.50	unknown	via CMAUP database
Bruceanic Acid F	70681803	Click to see CC(=CC(=O)OC1C2C34COC2(C(C(C3C(C(CC4OC1=O)C(=O)C)(C)CC(=O)O)O)O)C(=O)O)C	510.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol	10231	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC	222.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines / Methoxypyrazines
Nocazine B	56600877	Click to see CN1C(=CC2=CC=C(C=C2)OC)C(=NC(=CC3=CC=CC=C3)C1=O)OC	348.40	unknown	https://doi.org/10.1248/CPB.44.2236
> Organoheterocyclic compounds / Furopyrans
(1S,2R,3R,4S,6R,7R,10R,11R,12R)-2,6,11,12-tetrahydroxy-4,10-dimethyl-4-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-9,14-dioxatetracyclo[8.4.0.03,7.07,11]tetradecan-13-one	10453339	Click to see CC1=CC(=O)OC1C2(CC(C34C2C(C5C(C3(C(C(=O)O5)O)O)(OC4)C)O)O)C	396.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
Ethyl 2-hydroxyquinoline-4-carboxylate	160782	Click to see CCOC(=O)C1=CC(=O)NC2=CC=CC=C21	217.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavone	10680	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2	222.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1007/BF02976372
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
Luteolin-7-O-galactoside	5488493	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Thevetiaflavone	5315202	Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,3,6-Tetragalloyl-beta-D-glucopyranose	5153644	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	788.60	unknown	https://doi.org/10.1248/CPB.44.2236
NP-003686	73178	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	788.60	unknown	https://doi.org/10.1248/CPB.44.2236
> Phenylpropanoids and polyketides / Tannins / Complex tannins
(1S,2S,20S,42S,46R)-46-[(3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone	101676951	Click to see C1C(C(OC2=C1C(=CC(=C2C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O	1206.90	unknown	https://doi.org/10.1248/CPB.35.602
Acutissimin A	16132408	Click to see C1C(C(OC2=C1C(=CC(=C2C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O	1206.90	unknown	https://doi.org/10.1248/CPB.35.602
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1R,2R,20R,37R,45S,46R,52S)-7,8,9,12,13,14,25,26,27,30,31,32,35,40,41-pentadecahydroxy-4,17,22,36,48,51-hexaoxo-3,18,21,38,47,50-hexaoxaundecacyclo[27.17.3.334,46.02,20.05,10.011,16.023,28.033,49.037,45.039,44.037,52]dopentaconta-5,7,9,11,13,15,23,25,27,29(49),30,32,34,39(44),40,42-hexadecaene-43-carboxylic acid	163195188	Click to see C1C2C(C3C4C5C6=C(C(=C(C=C6C(=O)O)O)O)OC57C(C(=C(C7=O)O)C8=C(C(=C(C(=C8C(=O)O3)C9=C(C(=C(C=C9C(=O)O2)O)O)O)O)O)O)C(=O)O4)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1056.70	unknown	https://doi.org/10.1248/CPB.45.1751
(1R,2R,20R,37R,53S,54S,60S)-7,8,9,12,13,14,25,26,27,30,31,32,35,40,46,47-hexadecahydroxy-3,18,21,38,49,55,58,62-octaoxatetradecacyclo[27.25.3.334,54.241,44.02,20.05,10.011,16.023,28.033,57.037,53.039,52.042,51.043,48.037,60]dohexaconta-5,7,9,11,13,15,23,25,27,29(57),30,32,34,39(52),40,42(51),43(48),44,46-nonadecaene-4,17,22,36,50,56,59,61-octone	163020885	Click to see C1C2C(C3C4C5C6=C(C(=C7C8=C6C(=O)OC9=C8C(=CC(=C9O)O)C(=O)O7)O)OC55C(C(=C(C5=O)O)C5=C(C(=C(C(=C5C(=O)O3)C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O)O)C(=O)O4)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1188.80	unknown	https://doi.org/10.1248/CPB.45.1751
(1R,2R,20R,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-hexadecahydroxy-15-[(1R,2R,20R,42R,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaen-46-yl]-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11(16),12,14,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone	163192175	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)C8=C(C(=C(C9=C8C(=O)OCC2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C4=C(C(=C(C(=C4C(=O)O3)C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C29)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1851.20	unknown	https://doi.org/10.1248/CPB.44.2236
(1R,2R,20R,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-hexadecahydroxy-15-[(1R,2R,20R,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaen-46-yl]-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11(16),12,14,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone	101998420	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)C8=C(C(=C(C9=C8C(=O)OCC2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C4=C(C(=C(C(=C4C(=O)O3)C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C29)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1851.20	unknown	https://doi.org/10.1248/CPB.44.2236
(1R,2R,20S,42S,46R)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-46-(6,7,13,14-tetrahydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaen-5-yl)-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone	163185565	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)C8=C(C(=C9C2=C8C(=O)OC3=C2C(=CC(=C3O)O)C(=O)O9)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1218.80	unknown	https://doi.org/10.1248/CPB.45.1751
(1S,2S,24R,25R,29S)-7,8,9,12,13,14,17,18,19,25,29-undecahydroxy-24-(hydroxymethyl)-3,23,26-trioxahexacyclo[13.10.3.12,6.05,10.011,28.016,21]nonacosa-5(10),6,8,11,13,15(28),16,18,20-nonaene-4,22,27-trione	102505445	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C5=C6C(=C(C(=C5O)O)O)C(C(C(C(C(OC2=O)CO)O)OC4=O)OC6=O)O	632.40	unknown	https://doi.org/10.1248/CPB.44.2236
1-Epi-castalagin	12302512	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1248/CPB.44.2236
3,4,5-trihydroxy-2-[(1R,2R,20S,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaen-46-yl]benzoic acid	163187061	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)C8=C(C(=C(C=C8C(=O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1086.70	unknown	https://doi.org/10.1248/CPB.45.1751
5-[(2R,3S,3aR,9bR)-2-[(1R)-1,2-dihydroxyethyl]-3,7,8,9-tetrahydroxy-5-oxo-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-6-yl]-6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione	10793860	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C6C(=C(C(=C5O)O)O)C7C(C(C(O7)C(CO)O)O)OC6=O)O)O)OC2=O	614.40	unknown	https://doi.org/10.1248/CPB.44.2236
5-[(2R,3S,4S,4aR,10bR)-3,4,8,9,10-pentahydroxy-2-(hydroxymethyl)-6-oxo-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-7-yl]-6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione	10770082	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C6C(=C(C(=C5O)O)O)C7C(C(C(C(O7)CO)O)O)OC6=O)O)O)OC2=O	614.40	unknown	https://doi.org/10.1248/CPB.44.2236
6,7,13,14-tetrahydroxy-5-[5,6,7-trihydroxy-1-oxo-3-[(1S,2R,3R)-1,2,3,4-tetrahydroxybutyl]isochromen-8-yl]-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione	10675279	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C(C(=C(C6=C5C(=O)OC(=C6)C(C(C(CO)O)O)O)O)O)O)O)O)OC2=O	614.40	unknown	https://doi.org/10.1248/CPB.44.2236
Castacrenin A	85270241	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C6C(=C(C(=C5O)O)O)C7C(C(C(O7)C(CO)O)O)OC6=O)O)O)OC2=O	614.40	unknown	https://doi.org/10.1248/CPB.44.2236
Castacrenin B	85262147	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C6C(=C(C(=C5O)O)O)C7C(C(C(C(O7)CO)O)O)OC6=O)O)O)OC2=O	614.40	unknown	https://doi.org/10.1248/CPB.44.2236
Castacrenin C	85228592	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C(C(=C(C6=C5C(=O)OC(=C6)C(C(C(CO)O)O)O)O)O)O)O)O)OC2=O	614.40	unknown	https://doi.org/10.1248/CPB.44.2236
Castacrenin D	131751205	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)C8=C(C(=C(C=C8C(=O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1086.70	unknown	https://doi.org/10.1248/CPB.45.1751
Castacrenin E	131751206	Click to see C1C2C(C3C4C5C6=C(C(=C(C=C6C(=O)O)O)O)OC57C(C(=C(C7=O)O)C8=C(C(=C(C(=C8C(=O)O3)C9=C(C(=C(C=C9C(=O)O2)O)O)O)O)O)O)C(=O)O4)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1056.70	unknown	https://doi.org/10.1248/CPB.45.1751
Castacrenin F	131751203	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)C8=C(C(=C9C2=C8C(=O)OC3=C2C(=CC(=C3O)O)C(=O)O9)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1218.80	unknown	https://doi.org/10.1248/CPB.45.1751
Castacrenin G	22834921	Click to see C1C2C(C3C4C5C6=C(C(=C7C8=C6C(=O)OC9=C8C(=CC(=C9O)O)C(=O)O7)O)OC55C(C(=C(C5=O)O)C5=C(C(=C(C(=C5C(=O)O3)C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O)O)C(=O)O4)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1188.80	unknown	https://doi.org/10.1248/CPB.45.1751
Castalin	99973	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C5=C6C(=C(C(=C5O)O)O)C(C(C(C(C(OC2=O)CO)O)OC4=O)OC6=O)O	632.40	unknown	https://doi.org/10.1248/CPB.44.2236
CID 12302513	12302513	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1248/CPB.45.1751 https://doi.org/10.1248/CPB.44.2236
CID 5458626	5458626	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1248/CPB.44.2236 https://doi.org/10.1248/CPB.45.1751
CID 72679636	72679636	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)C8=C(C(=C(C9=C8C(=O)OCC2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C4=C(C(=C(C(=C4C(=O)O3)C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C29)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1851.20	unknown	https://doi.org/10.1248/CPB.44.2236
Vescalagin	168165	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1248/CPB.45.1751 https://doi.org/10.1248/CPB.44.2236
Vescalin	15698968	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C5=C6C(=C(C(=C5O)O)O)C(C(C(C(C(OC2=O)CO)O)OC4=O)OC6=O)O	632.40	unknown	https://doi.org/10.1248/CPB.44.2236

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Castanea crenata

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